Di Monaco M, Pizzini A, Gatto V, Leonardi L, Gallo M, Brignardello E, Boccuzzi G
Department of Clinical Pathophysiology, University of Turin, Italy.
Br J Cancer. 1997;75(4):589-92. doi: 10.1038/bjc.1997.102.
Epidemiological and experimental studies suggest that dehydroepiandrosterone (DHEA) exerts a protective effect against breast cancer. It has been proposed that the non-competitive inhibition of glucose-6-phosphate dehydrogenase (G6PD) contributes to DHEA antitumor action. We evaluated the effects of DHEA on G6PD activity and on the in vitro proliferation of two human breast cancer cell lines, MCF-7 (steroid receptor positive) and MDA-MB-231 (steroid receptor negative), in a serum-free assay. DHEA inhibition of G6PD was only found to occur at concentrations above 10 microM; at these high concentrations, the growth curve was parallel to the enzyme inhibition curve in both cell lines. In contrast, at concentrations in the in vivo breast tissue concentration range, neither cell growth nor enzyme activity was inhibited. The results failed to confirm DHEA's putative anti-tumor action on breast cancer through G6PD inhibition, as the enzyme blockade only becomes apparent at pharmacological concentrations of the steroid.
流行病学和实验研究表明,脱氢表雄酮(DHEA)对乳腺癌具有保护作用。有人提出,葡萄糖-6-磷酸脱氢酶(G6PD)的非竞争性抑制作用有助于DHEA的抗肿瘤作用。我们在无血清试验中评估了DHEA对G6PD活性以及两种人乳腺癌细胞系MCF-7(类固醇受体阳性)和MDA-MB-231(类固醇受体阴性)体外增殖的影响。仅在浓度高于10微摩尔时才发现DHEA对G6PD有抑制作用;在这些高浓度下,两种细胞系的生长曲线均与酶抑制曲线平行。相反,在体内乳腺组织浓度范围内的浓度下,细胞生长和酶活性均未受到抑制。结果未能证实DHEA通过抑制G6PD对乳腺癌具有假定的抗肿瘤作用,因为只有在该类固醇的药理浓度下酶阻断作用才会明显显现。